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Celiac.com Article: Patients with Active Celiac Disease At Slightly Higher Risk for Eosinophilic Esophagitis


Jefferson Adams

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  • Recent Activity

    1. - Aretaeus Cappadocia replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
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      1 Year Elimination Diet journey

    2. - trents replied to lehum's topic in Super Sensitive People
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      4.5 years into diagnosis, eating gluten-free and still struggling: would love support, tips, & stories

    3. - Heatherisle replied to Mihai's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
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      Pain in the right side of abdomen

    4. - dixonpete commented on dixonpete's blog entry in Pete Dixon
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      Another conversation with ChatGPT about hookworms

    5. - Scott Adams commented on dixonpete's blog entry in Pete Dixon
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      Another conversation with ChatGPT about hookworms

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    • Aretaeus Cappadocia
      I love buckwheat groats (or kasha). I also like to add peanut butter to it. There are a bunch of these alternatives but I also recommend amaranth. It's good with fruit and/or cinnamon.
    • trents
      @nancydrewandtheceliacclue, if you had trouble breathing, I agree with Scott. That sounds like anaphylaxis. 
    • Heatherisle
      Hi  Sorry not been on for a while. My daughter had a recent hospital stay as went to GP with slight blurred vision, lower back pain and tingling in hands and feet, slight balance problems. GP wanted to rule out stroke. Had recently started Vit B12 medication as blood test showed really low level of 30, folate was 2.2. Was admitted for 4 days, various tests including head CT ruled out stroke but was commenced on B12 injections instead of tablets. Had follow up MRI 5 weeks ago and she is now being referred to neurology as possible transient lesion seen on frontal lobe, so something else to worry about. Hoping it’s all connected to her B12 levels. Her tingling seemed to settle after getting injections 3 times/ week for two weeks and has just had her 2nd monthly dose but a week late and felt the tingling coming back just before that.Just wondering if anyone else has experienced this.  Thanks for reading and sorry to be a pain!!!!
    • xxnonamexx
      It has been a year since I started my Elimination diet from gluten. I have learned alot w/o being diagnosed (going through eating gluten for a test isn't happening) The first month or so were learning curve and I have learned to READ LABELS which are tricky as not just gluten but possibly wheat may affect you or other Gluten containing ingredients that are spelled out. I have found great protein bars w/o sugar alcohols as I noticed those increased gas. I have taken vitamins as suggested by members on this board. Started baking gluten free, when going out I have found gluten friendly restaurants. I have felt so much better since eliminating gluten/sugar alcohols. It is hard to find sugar free products but I limit myself to gluten free snacks as they have high sugar etc. I have been using Bobs Red Mill gluten-free oatmeal and One Degree Farmers oatmeal but I am looking to try some new breakfast ideas like Buckwheat or a great gluten-free cereal. Journey still continues and learning more and more.
    • Scott Adams
      It may help to bring the clearest photos, avoid squeezing or digging at the bumps, and ask your doctor whether a skin scraping, culture, biopsy, or parasite/fungal evaluation would be appropriate based on what they see. Since you mentioned cats, it’s also worth asking about possible flea bites, mites, ringworm, or other pet-related skin issues, and checking with a veterinarian if your cats have itching or hair loss. Also, please tell your doctor about the topiramate change, meningioma, and the garlic, especially since you were told not to eat garlic. Even if your husband doesn’t see what you see, your symptoms are real and deserve a careful medical evaluation.
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